A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977624



Internal ID22752559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:113202020..113214744hg38UCSC Ensembl
chrX:112445247..112457971hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3812725
hg1912725
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515145
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977624
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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